Nanomedicine: An Innovative Approach Towards Treating ... · Nanomedicine: An Innovative Approach Towards Treating Tuberculosis. H. SWAI. 1, L. KALOMBO, B. SEMETE and L. KATATA ...

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Polymericshell

Nanomedicine: An Innovative Approach Towards Treating Tuberculosis

H. SWAI1, L. KALOMBO, B. SEMETE and L. KATATA

Encapsulation and Delivery Research GroupPolymers and Composites,

Materials Science and Manufacturing *E-mail: [email protected], +27 12-841-2366

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TB: Prevalence in South AfricaSouth Africa TB StatisticsTB leading cause of death in SA

Highest infection rate in Africa

Fourth highest in the world

Due to:

Co-infection of HIV and TB in 80% of cases

Patients non compliance

Poor bioavailabilityTreatment period (6-9 months)

Dose and dose frequency

Adverse side effect

Hence

Multi-drug resistant TB (MDR-TB)

Extremely resistant TB (XDR-TB)

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Conventional Oral Delivery SystemLimiting factors for oral delivery• Gastric Intestinal Track (GIT):

• Harsh environment• Bioactives degradation• Poor permeability• Relatively short gastric

emptying and intestinal transit time

• Pre-systemic clearance

• Hence:• Poor bioavailability

• Increased dose & dose frequency

• Increased length of treatment• Drug toxicity• Drug-drug interaction

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Nano encapsulated TB drugs

Anti-TBdrugs

Polymericshell

INH-loaded PLGA nanoparticles

1 um

CLSM image of macrophage cell taken up 1 um size particles

200 nm

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Nanodrug delivery system in the GIT

Structure of the GIT Internal structure of the intestine

• Para-cellular via M cell

• Intracellular via epithelial cell-intestine mucosa

• Peyer's patches

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Routes and mechanisms of particle transport across epithelia

DC

UPTAKE via MALT

Lymph capillary

SER

OSA

L SI

DE

MU

CO

SAL

SID

E

mucus

Epithelial

cell

Celljunctio

n

ENDOCYTOSISby ordinary enterocytes

PARACELLULAR

LNBlood circulation

blood capillary

• Modified surface• Increase circulation time: PEG• Enhance particle uptake: Chitosan

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First pass metabolism 

Metabolism

AbsorptionDose

Excretion

Distribution 

Nanoparticle Transport

Roslyn Thelingwani

Spleen

Entry into lymphatic system

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Promises of Nano-drug delivery

• Enhance anti-TB drug properties• Solubility • Rate of dissolution: sustained and controlled release systems• Oral bioavailability: minimise first pass metabolism• Targeting ability

• Enhance anti-TB drug dosing requirements • Reduced dose and dose frequency• Minimal adverse side effects• Shortened treatment time • Improve patient compliance

• Generic (platform) technology • Anti-malarials• ARVs• Anti-cancer drugs• Long term pain killers• Traditional medicines

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Proposed Solution

• Encapsulation of ATDs into multifunctional polymeric nanoparticles.

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Hydrophilic drug

Hydrophobic drug

Muco-adhesive ligand

Stealth coating

Targeting ligand

Schematic diagram of a multifunctional polymeric nanocarrier

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Project technical status

• Successfully nano encapsulated 4 of first line anti-TB drugs • Using double emulsion solvent evaporation - spray drying technique • PCT patent application filed

• Properties:• 200 nm average size• Highly reproducible production• Scalable (known pharmaceutical process equipment)• Narrow size distribution (polydispersity < 0.1)• Controllable surface charge• Modified surface

• Increase circulation time: PEG• Enhance particle uptake: Chitosan

• Developed other encapsulations systems• Natural polymers • Other synthetic polymers (Polycaprolactone)• Establishing a drug delivery platform

• ARVs• Malaria• Other PRD’s

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Encapsulation of all four drugs• Encapsulation of pre-formed drug-loaded micelle-like

containers

PLGA Nanocapsule

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In vitro uptake in CaCo-2 cells

Z-stack 30 min incubation 60 min incubation

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In vitro uptake in THP-1 cells

a) Coumarin labelled b) INH-PLGA

c) Rhodamine labelled

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Tissue distribution of Rhodamine labelled PLGA nanoparticles after 1 day exposure (CLSM images)

LUNGS LIVER KIDNEY

SPLEEN BRAIN HEART MUSCLES

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Tissue sections : High dose of PLGA particles

BRAIN

KIDNEY

HEART MUSCLES

LIVERLUNG

SPLEEN

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Release profile for free drugs vs encapsulated drugs: Improved formulation (Swai et al. unpublished data)

IN VIVO release

0.01

0.1

1

10

100

0 20 40 60 80 100 120 140 160

Hours

Con

c (u

g/m

l)

INH -2

INH-1

INH multi-drugs

Conv-INH

MIC-INH

RIF1

RIF2

Conv Rif

MIC-RIF

RIF Multidose

PZA1

PZA2

Conv-PZA

PZA Multidose

MIC-PZA

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Progress summary• Encapsulated 4 first line ATDs

• PCT patent filed- double emulsion SD technique • Micelles • Natural Polymers• 2 further invention disclosures

• In vitro assays • In vitro efficacy• In vitro stability and slow release profile• Particle uptake

• In vivo assays• Macrophage uptake• No abnormalities in tissues• No inflammatory response• Sustained release profile over 6 days

• Generic technology• Anti-retrovirals, antibiotics etc. • In search of collaborators in Malaria and traditional actives

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Active targeted drug delivery

• Inherent macrophage mechanisms being manipulated- Phagocytosis and endocytosis- Over expression of protein in TB infected macrophages

• Direct mannose receptor mediated particle uptake• Novel technology• Aptamers against target protein• Preferential localization of particles

• Macrophage over expressing protein

• Mycolic acid• Cell wall of M.tb• Directing nanoparticles to M.tb in cells

Single stranded RNA

Folding

Incubation with target protein

Molecular complex

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Overview of drug delivery platform relationships & agreements

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Progress on HR Capacity Building• Recruitment progress

• 4 Post docs - Boitumelo Semete, Paul Chelule and Malebogo Legodi, Lebogang Katata

• 4 PhD students –Yolandy Benadie, Lonji Kalombo, Lindiwe Nkabinde and Laetitia Booysen

• 3 MSc students – Phumzile Hadebe, Saloshnee Naidoo and Trudy Maluleke• 4 Technikon students - Sonia Mathopo, Batabile Ramalapa and Koketso

Rapatla and Mofahloshi Chuene• Training completed (2006-2008)

• University of London, UK• EPFL, Switzerland • PGIMER, Chandigarh, India. • University of Nottingham, UK • University of Cardiff, UK• University of Liverpool, UK

• Training arranged for 2009 onwards• National Jewish Medical and Research Centre, USA • University of Nottingham, UK• University of London, UK• University of Colorado, USA

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THANK YOU

TB Nanodrug delivery Research Team - CSIR